NDC 70518-4239 – Escitalopram
Escitalopram Oxalate 20 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-4239
Product details
- Brand name
- Escitalopram
- Generic name
- Escitalopram
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078777
- Marketed since
- December 13, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Escitalopram Oxalate 20 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 70518-4239-0 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4239-0) | Dec 13, 2024 |
| 70518-4239-1 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-1) | Feb 25, 2025 |
| 70518-4239-2 | 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-2) | Jun 19, 2025 |
| 70518-4239-3 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-3) | Jul 1, 2025 |
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